SCANLAN® Instrumentation CDA002-RS

GUDID 00846159035858

SCANLAN® Retractor Blade

SCANLAN INTERNATIONAL INC

Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable

• Primary Device ID: 00846159035858
• NIH Device Record Key: 3408a543-770b-4958-aff7-d60b22fc27e5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCANLAN® Instrumentation
• Version Model Number: CDA002-RS
• Catalog Number: CDA002-RS
• Company DUNS: 023055619
• Company Name: SCANLAN INTERNATIONAL INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846159035858 [Primary]

FDA Product Code

• GAD: Retractor

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

[00846159035858]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-08-17
• Device Publish Date: 2022-08-09

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